Le Chatlier's Principle Flashcards

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1
Q

In a reaction, if you increase the pressure or decrease volume, the rxn will move toward the side with more or less moles?

A

Less moles. By increasing the pressure, the rxn will want to balance out and this can be achieved by heading in the direction of the rxn that has less moles.

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2
Q

In a reaction, if you decrease the pressure or increase the volume of one side, will the reaction move toward the side with more or less moles of gas?

A

It would move toward the side with more moles to compensate.

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3
Q

Changes in temperature, if you increase the temperature , the reaction will move toward what side ?

A

The reaction will favor the side in which heat is not a part of.

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4
Q

If you decrease the temperature of a reaction, what side will the reaction move toward?

A

It will favor the side of the reaction that generates heat to compensate

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5
Q

If reactants are added or products are removed

A

Q

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6
Q

If reactants are removed or products are added

A

Q > Keq

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7
Q

Enthalpy

A

Heat changes at constant pressure. It is a state function. All we need to do is compare the final and initial state. A positive dH value is endothermpic (breaking bonds). -dH means reaction is exothermic (Forming bonds)

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8
Q

You cannot determine spontaneity from

A

Enthalpy. You can determine it from Gibbs Free Energy ONLY!

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9
Q

Standard Enthalpy (Heat) of Formation

A

Enthalpy requuired to produce one mole of a compound from its elements in their standard states. 298 K or 25 Celcius and 1 atm. Do not assume standard state is a common state.

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10
Q

Standard Heat of Reaction:

A

This is a state function, so subtract - final- initial. Only can do this if we know what the heat of formation of the compounds are.

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11
Q

Hess’s Law

A

States that enthalpy of a reaction is a sum of each reaction. Basically say that there are several intermediates, but if we add the steps together we can get the total. It applies really to all of the state functions.

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12
Q

Bond Dissociation Energy

A

Average energy required to break a bond, expect the units to be in kJ/mol. All bond dissociation energies are endothermic. If we use this we just take the total enthalpy of bonds broken- bonds formed. You can look at this as total energy absorbed - total energy released. This breaks the general trend because it is going from initial-final and not final- initial.

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13
Q

The heat of combustion will always have a - or + dH rxn?

A

-dH rxn

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14
Q

A positive H is

A

endothermic

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15
Q

A negative H is

A

exothermic

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16
Q

The Second Law of Thermodynamics deals with

A

Entropy. Work must be applied for energy to move from a diffuse to a more localized state.

17
Q

Entropy

A

Measure of spontaneious disperal of energy at a specific temperature. dS= Q(heat gained or lost)/ T ( in Kelvin). Heat energy into a system (entropy increases). If we take heat energy out of a system (entropy decreases).

18
Q

Entropy Equations

A

Entropy universe= Entropy of system + Energy of surroundings >0

Standard Entropy (state function, pathway independent, final and initial state is all that matters)
dS rxn = Summ of dS products - dS reactants
19
Q

By decreasing activation energy of the reaction , what effect is produced on equilibrium constant?

A

nothing it stays constant. Only temperature can change the equilibrium constant

20
Q

State functions

A

gibbs, entropy , enthalpy and volume change

21
Q

catalyst

A

decreases activation energy AND is regenerated

22
Q

Grahams Law

A

Kinetic Energy of Ideal Gases= 3/2nRT. It means that gases at the same temperature have the same kinetic energy.

23
Q

Ideal Behavior Includes

A

No intermolecular forces, No volume of particles